| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3157521-3157688 | Common:6; Rare:59 | ||||
| chr6:3258818-3259026 | Rare:82 | ||||
| chr6:4021209-4021437 | Rare:102 | ||||
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5004007-5004112 | Common:1; Rare:51 | ||||
| chr6:5260691-5261025 | Common:3; Rare:111; Clinvar (benign):4 | ||||
| chr6:5261282-5261553 | Common:9; Rare:62 | ||||
| chr6:7313127-7313404 | Common:4; Rare:99 | ||||
| chr6:7389753-7389986 | Common:1; Rare:57 | ||||
| chr6:7541359-7541748 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:7541789-7542074 | Common:4; Rare:109; Clinvar:14; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr6:7910586-7910944 | Common:4; Rare:142 | ||||
| chr6:8064327-8064632 | Common:4; Rare:92 | ||||
| chr6:8435330-8435669 | Common:5; Rare:116 | ||||
| chr6:10412164-10412308 | Rare:50 |